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Recall totals

All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.

37,139

Total recall recordsAll FDA and USDA recalls in Public Health Trace

9,799

Class I recallsReasonable probability of serious health consequences

24,349

Class II recallsTemporary or medically reversible health consequences

2,891

Class III recallsNot likely to cause adverse health consequences

Quick insights

A snapshot of the most notable patterns across all recorded FDA and USDA recalls.

Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap. 53 recalls

Most common hazardLack of Assurance of Sterility 2,072 recalls

Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/deanos-pasta-issue-allergy-alert-undeclared-lobster-pear-and-pecorino-triangoli-ravioliPublished September 24, 2026

Most affected stateHawaii 200 recalls mention this state

State: WA ×
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Recalls announced by month (Year to date)

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Source: FDA and USDA public dataLast updated September 25, 2026 ET

Summary (Year to date)

1,527 recalls have been announced year to date.
Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
The highest complete period was Jun 2026 (297).
Sep 2026 is incomplete and not included in the figures above.

Complete data
Incomplete

Recalls by class

Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

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Recalls by class
Class	Recalls
Class II	24,349
Class I	9,799
Class III	2,891
Not Yet Classified	1

FDA Recall Terminated Historical recordClass III

TESTOSTERONE 200 mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-120-01

by Qualgen, LLC

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date.
Published: July 11, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

ESTRADIOL 20mg PELLET, 1-count 3ml amber vial. RX only. Compounded by: Qualgen 14844 Bristol Park Blvd, Edmond OK 73013. NDC 69761-020-01

by Qualgen, LLC

Reason: Labeling: Incorrect or Missing Lot and/or Exp Date.
Published: July 11, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Irinotecan Hydrochloride Injection, USP, 40 mg/2 mL (20 mg/mL), 1 x 2 mL Single Dose Vial, Rx Only, Manufactured for: Ingenius Pharmaceuticals, LLC, Orlando, FL 32839-6408; Manufactured by: Ingenius Pharmaceuticals, GmbH Ticino 6917, Switzerland, NDC 50742-401-02.

by Ingenus Pharmaceuticals Llc

Reason: Superpotent Drug: High out of specification assay value results for potency.
Published: July 11, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

Irinotecan Hydrochloride Injection, USP, 100 mg/5 mL (20 mg/mL), 1 x 5 mL Single Dose Vial, Rx Only, Manufactured for: Ingenius Pharmaceuticals, LLC, Orlando, FL 32839-6408; Manufactured by: Ingenius Pharmaceuticals, GmbH Ticino 6917, Switzerland, NDC 50742-402-05.

by Ingenus Pharmaceuticals Llc

Reason: Superpotent Drug: High out of specification assay value results for potency.
Published: July 11, 2018
Distribution: Nationwide

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FDA Recall United States Terminated Historical recordClass II

Icelandic Provisions Inc.

Product: Icelandic Provisions Vanilla Skyr cups, 5.3oz package, UPC:…
Reason: Cups containing coconut skyr yogurt may have been mislabeled as vanilla skyr yogurt.
Published: July 11, 2018
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass III

Supreme Foods

Product: Pacific Brand Charcoal Grilled Eel. Premium Quality Unagi K…
Reason: FDA Compliance follow-up inspection found that imported shipments of eel on import alert that should have been held had been distributed. FDA found Mebendazole amine in two of the shipments.
Published: July 4, 2018
Distribution: Multiple states

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FDA Recall United States Terminated Historical recordClass I

New Seasons Market LLC

Product: Mini Butter Croissants, 8-Pack, packaged in a clear plastic…
Reason: Mini Butter Croissants are recalled because the Ingredients statement and Contains statement do not declare EGG.
Published: July 4, 2018
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass III

New Seasons Market LLC

Product: Vegan Chocolate Almond Muffin, 4-pack, packaged in a clear c…
Reason: Vegan Chocolate Almond Muffin is recalled because the Contains statement does not declare ALMOND.
Published: July 4, 2018
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

New Seasons Market LLC

Product: Blueberry Buckwheat Muffin, 4-pack, packaged in a clear clam…
Reason: Blueberry Buckwheat Muffin is recalled because the Contains statement does not declare EGG.
Published: July 4, 2018
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass III

New Seasons Market LLC

Product: Honey Oat Bran Muffin, 4-pack, packaged in a clear clamshell…
Reason: Honey Oat Bran Muffin is recalled because the Contains statement does not declare EGG.
Published: July 4, 2018
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass I

New Seasons Market LLC

Product: Mini Chocolate Croissants, 8-Pack, packaged in a clear plast…
Reason: Mini Chocolate Croissants are recalled because the Ingredients statement and Contains statement do not declare EGG. In addition, Mini Chocolate Croissants are recalled because the Contains statement does not declare SOY LECITHIN.
Published: July 4, 2018
Distribution: Distributed in OR and WA

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FDA Recall United States Terminated Historical recordClass II

New Seasons Market LLC

Product: Meyer Lemon Chia Muffin, 4-pack, packaged in a clear clamshe…
Reason: Meyer Lemon Chia Muffin is recalled because the Contains statement does not declare EGG.
Published: July 4, 2018
Distribution: Distributed in OR and WA

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium Tablets, 40 mg*, packaged as a) 90-count bottle (NDC 55111-123-90 and b) 500-count bottle (NDC 55111-123-05), Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium Tablets, 20 mg*, 90-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-122-90

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass III

Atorvastatin Calcium Tablets, 10 mg*, 90-count bottle, Rx Only, Mfd. By: Dr. Reddy's Laboratories Limited, Srikakulam - 532 409 INDIA, NDC 55111-121-90

by Dr. Reddy's Laboratories, Inc.

Reason: Failed Impurities/Degradation Specifications
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

5% Dextrose Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7922-02

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection, USP, 100 mL bag, Rx Only ,Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7984-37

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection, USP, 100 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7984-23

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.9% Sodium Chloride Injection, USP, 250 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7983-02

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

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FDA Recall Terminated Historical recordClass II

0.45% Sodium Chloride Injection, USP, 100 mL bag, Rx Only, Hospira, Inc. Lake Forest, IL 60045, NDC 0409-7730-37

by ICU Medical Inc

Reason: Lack of assurance of sterility: Bags have potential to leak.
Published: June 27, 2018
Distribution: Nationwide

View recall →

Data last updated: September 25, 2026 ET

Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.